| Weight | 181.238 g/mol |
|---|---|
| Formula | C13H11N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
Benzophenone imine (1013-88-3)
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- Theoretical studies in molecular recognition : asymmetric induction of benzophenone imine ester enolates by the benzylcinchoninium ion (Journal of Organic Chemistry, 1991)
- First example of the solid-state thermal cyclometalation of ligated benzophenone imine giving novel luminescent platinum(II) species (Inorganic Chemistry, 2007)
- Imine containing benzophenone scaffold as an efficient chemical device to detect selectively Al3 (RSC Advances, 2013)
- Displacement of Phenyl and Styryl Ligands by Benzophenone Imine and 2-Vinylpyridine on Ruthenium and Osmium (Organometallics, 2006)
- Synthesis and Reactivity of Triruthenium Carbonyl Cluster Complexes Containing a Bridging 1-Azavinylidene Ligand Derived from Benzophenone Imine (Organometallics, 1996)
- Cinchona alkaloid-based polymer-bound phase-transfer catalysts: efficient enantioselective alkylation of benzophenone imine of glycine esters. (Molecular Diversity, 2005)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)C(=N)C2=CC=CC=C2
-
InChIKeySXZIXHOMFPUIRK-UHFFFAOYSA-N
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Benzophenone imine
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